2016
DOI: 10.3109/09513590.2015.1121982
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Dydrogesterone use in early pregnancy

Abstract: Successful oocyte implantation and a favorable pregnancy outcome rely on optimal progesterone levels. Therefore, progesterone deficiencies associated with infertility and miscarriage have commonly been treated with progestogens that mimic the activity of progesterone. Among those is dydrogesterone, an oral retrosteroid with a structure closely related to that of progesterone yet with a greater bioavailability and higher selectivity for the progesterone receptor. This review describes the efficacy of dydrogeste… Show more

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Cited by 54 publications
(33 citation statements)
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“…Compared with progesterone, dydrogesterone has a greater affinity for the progesterone receptors and can be used at lower oral doses to promote endometrial proliferation, owing to its better bioavailability and to the progestogenic activity of its metabolites (Schindler et al ., 2008). Dydrogesterone also appears to have no affinity for androgenic, estrogenic, glucocorticoid or mineralocorticoid receptors (Schindler, 2009), demonstrating a favorable safety and tolerability profile in pregnancy, both to the mother and child (Queisser-Luft, 2009; Mirza et al ., 2016). Furthermore, data from prospective trials for luteal phase support in IVF show that oral dydrogesterone is as effective as micronized vaginal progesterone (MVP), is well tolerated overall, and has a higher patient satisfaction rate than MVP (Chakravarty et al ., 2005; Patki and Pawar, 2007; Ganesh et al ., 2011; Salehpour et al ., 2013; Tomic et al ., 2015; van der Linden et al ., 2015; Saharkhiz et al ., 2016).…”
Section: Introductionmentioning
confidence: 99%
“…Compared with progesterone, dydrogesterone has a greater affinity for the progesterone receptors and can be used at lower oral doses to promote endometrial proliferation, owing to its better bioavailability and to the progestogenic activity of its metabolites (Schindler et al ., 2008). Dydrogesterone also appears to have no affinity for androgenic, estrogenic, glucocorticoid or mineralocorticoid receptors (Schindler, 2009), demonstrating a favorable safety and tolerability profile in pregnancy, both to the mother and child (Queisser-Luft, 2009; Mirza et al ., 2016). Furthermore, data from prospective trials for luteal phase support in IVF show that oral dydrogesterone is as effective as micronized vaginal progesterone (MVP), is well tolerated overall, and has a higher patient satisfaction rate than MVP (Chakravarty et al ., 2005; Patki and Pawar, 2007; Ganesh et al ., 2011; Salehpour et al ., 2013; Tomic et al ., 2015; van der Linden et al ., 2015; Saharkhiz et al ., 2016).…”
Section: Introductionmentioning
confidence: 99%
“…Additional evidence for an upstream role of progesterone in ameliorating the risk for pregnancy pathologies arise from more recent studies on progestogens supplementation during early pregnancy (3,106,107). Reduced progesterone, e.g., due to luteal insufficiency or stress may influence maternal tolerance toward fetal antigens and result in fetal loss (108,109).…”
Section: Progesterone Infertility and Early Pregnancy Lossmentioning
confidence: 99%
“…But the safety of pharmacology for embryos in the case of MPA has not been confirmed. On the other hand, DYG is widely used as a treatment for improving pregnancy outcomes in women with threatened miscarriage (Howard et al, 2012;Mirza et al, 2016;Rizner et al, 2011). Previously, our clinic also prescribed DYG for PPOS.…”
Section: Main Findingsmentioning
confidence: 99%